Case Series Study of Biliary Tract Cancer Patients in Japan

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Brief Title

Case Series Study of Biliary Tract Cancer Patients in Japan

Official Title

Retrospective Analysis of the Difference of Prognosis Between Unresectable and Recurrent Biliary Tract Cancer

Brief Summary

      To assess the difference of prognosis between unresectable and recurrent biliary tract cancer
      and evaluate prognostic factors.
    

Detailed Description

      Most patients of biliary tract cancer have advanced disease at diagnosis and often relapse
      despite surgery. Combination therapy of gemcitabine and cisplatin could be a standard therapy
      for this kind of cancer with the evidence of phase III study compared with gemcitabine alone.
      However the prognosis and the tolerability of chemotherapy in the patients with recurrent
      biliary tract cancer after radical resection might differ from those of unresectable biliary
      tract cancer, because the dose intensity of chemotherapy can be influenced by adjuvant
      chemotherapy and/or hepatic resection.
    


Study Type

Observational


Primary Outcome

One year survival rate

Secondary Outcome

 Overall survival time

Condition

Biliary Tract Cancer



Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information



Estimated Enrollment

300

Start Date

November 2010

Completion Date

August 2011

Primary Completion Date

February 2011

Eligibility Criteria

        Inclusion Criteria:

          -  Unresectable or recurrent biliary tract cancer

        Exclusion Criteria:

          -  None
      

Gender

All

Ages

20 Years - N/A

Accepts Healthy Volunteers

No

Contacts

Tatsuya Ioka, MD, , 

Location Countries

Japan

Location Countries

Japan

Administrative Informations


NCT ID

NCT01294085

Organization ID

KHBO1001

Secondary IDs

UMIN000004530

Responsible Party

Sponsor

Study Sponsor

Kansai Hepatobiliary Oncology Group


Study Sponsor

Tatsuya Ioka, MD, Study Director, Osaka Medical Center for Cancer and CVD


Verification Date

November 2011